Primer for silicone substrates

ABSTRACT

A primer composition, and a method for its use to improve adhesion between a silicone substrate and a subsequently applied paint film, is disclosed. The primer composition consists essentially of a mixture of an alkoxysilane, an organotitanate and a tin salt of a carboxylic acid, each component being present in a specific critical molar proportion.

FIELD OF THE INVENTION

The present invention relates to a primer composition for siliconesubstrates and a method for its use to improve adhesion between theprimed substrate and a subsequently applied overcoat or paint film. Moreparticularly, the invention relates to a primer composition consistingessentially of a mixture of an alkoxysilane, an organotitanate and a tinsalt of a carboxylic acid, each component being present in a specificcritical proportion.

BACKGROUND OF THE INVENTION

Various substrates, such as metals, glass and plastics, require theapplication of a primer before they can be coated with a conventionalpaint or other coating formulation. Such primer compositions have oftenrelied on one or more organosilane compounds to promote the adhesionbetween substrate and coating. Thus, for example, Finzel, in U.S. Pat.No. 4,654,236, teaches a method for priming coil coated substrates witha solution of a tetraorganosilane and a tetraalkyltitanate. The primedsurfaces can be subsequently painted to provide surfaces which are asdurable as the original coil coatings. Similar organosilanes can also beemployed in various compositions for purposes other than primingsubstrates. For example, U.S. Pat. No. 4,846,886 to Fey et al. disclosescompositions wherein an improved water repellent composition for poroussubstrates is formed from an alkylalkoxysilane, a carrier, a waterbeading agent and a metal salt catalyst.

Of concern herein is the particular difficulty of painting orovercoating a silicone substrate. This operation is particularlytroublesome since silicone and silicone polymer substratescharacteristically exhibit very low surface energies. They are thusbetter known in the art for their abhesive nature and typically tend torelease most coating compositions applied thereto. Since it is oftendesirable to paint or otherwise overcoat a silicone substrate (e.g., fordecorative purposes. abrasion/erosion resistance, printing, marking)many attempts have been made over the years to develop satisfactoryprimers for this application. The following disclosures represent therelevant art of this type known to applicant.

Young, in U.S. Pat. No. 3,671,483, discovered that a solution containinga tetraalkyltitanate and a particular silane which has at least onegroup of the formula --CH₂ CH₂ --Si(OOCCH₃)₃ in its molecule is usefulas a primer in adhering a silicone rubber to epoxy and polyurethane.

In U.S. Pat. No. 3,677,998, Young also teaches that a solution of anorganotitanate, tetra(methoxyethoxy)silane, a methylsiloxane resin andeither acetic acid or an organotriacetoxysilane is useful as a primer inadhering a silicone rubber to a metal surface.

Hirai et al., in U.S. Pat. No. 4,598,134, teach a primer composition forheat curable silicone rubber consisting essentially of at least oneepoxy-functional organosilicon compound, a trialkoxysilane having eithertwo silicon-bonded hydrogens or two unsaturated groups or a partialhydrolyzate of said trialkoxysilane, and an organotitanate ester.

Saito et al., in U.S. Pat. No. 4,681,636 disclose a primer compositionparticularly suitable for bonding fluorosilicone rubber to a substrate.This primer comprises a solution of a t-butyl peroxy-functional silane,a reactive organosilicon compound having at least two alkoxy groups andan organotitanate ester. In another disclosure to Saito et al., U.S.Pat. No. 4,749,741, primers suitable for promoting adhesion betweensilicone rubber and plastics or metals are taught. These primers aresimilar to their previous systems and comprise a solution of anunsaturated organotitanate ester and either an organosilicon compoundhaving at least two alkoxy groups or an organohydrogensiloxane (orsilane).

In U.S. Pat. No. 4,704,419, Fukayama et al. teach primer compositionswhich improve adhesion of paints to cured silicone rubber and comprise asolution of an amine-functional dialkoxysilane and a liquid hydroxylterminated polyorganosiloxane, optionally further comprising a catalyst.

Meddaugh, in U.S. Pat. No. 4,923,946, discloses a primer formoisture-cured silicone sealants which imparts paintable surfacesthereto. The primers disclosed contain a solution of a hydrolyzate of anaminoalkyl-substituted trialkoxysilane and a carboxylic acid salt oftin.

A method for bonding to a silicone rubber is disclosed in Japanese KokaiPatent No. 59[1984]-48768 to Toray Industries, Inc. Here, a waterlesslithographic plate having a photosensitive layer, an adhesive layer anda silicone rubber layer is described wherein the adhesive layer containsan organic titanate. Printing plates of this invention are stated have astrong adhesion between the photosensitive layer and the silicone rubberlayer.

In addition to the above described art, the following United Statespatents teach various primer compositions which promote adhesion tosilicone surfaces: 4,431,472 to Hohl et al., 4,122,127 to Mikami et al.,4,534,815 to Hamada et al., 4,546,018 to Ryuzo et al., 4,133,938 toBingham, 4,147,685 to Smith, 4,332,844 to Hamada et al., 3,619,256 toPepe et al., 4,808,483 to Nakasuji et al., 4,436,787 to Mikami et al.and 4,401,500 to Hamada et al.

SUMMARY OF THE INVENTION

It has now been found that certain blends of an alkoxysilane, anorganotitanate and a tin salt of a carboxylic acid can act as a superiorprimer composition for certain silicone substrates which aresubsequently to be overcoated or painted with a silicone or organiccomposition, thereby providing greatly improved adhesion between thesilicone substrate and the overcoat film. Surprisingly, it has beenobserved that this marked improvement in adhesion is obtained only whenthe above named components are present in the critical molar ratiosdescribed infra. Thus, for example, a preferred water repellantcomposition disclosed by Fey et al., cited supra, consists of 85 weightpercent isobutyltrimethoxysilane, 10 weight % tetraisopropyltitanate and5 weight % dibutyltindilaurate. This composition, although similar tothe primers of the instant invention, is not within the critical rangediscovered by applicant and has not been found to be an effective primerfor silicone substrates. More to the point, Fey et al. do not suggestthe use of their water repellant compositions as primers for siliconesubstrates. It is thus the discovery of the use of such narrowly definedcompositions to prime certain silicone substrates, and the discovery ofthe apparently synergistic range of the necessary ingredients, which isat the heart of the present invention.

The instant invention therefore relates to a primer compositionconsisting essentially of a mixture of (I) from 25 to 75 mole percent ofat least one alkoxysilane having the general formula

    R.sub.x Si(OR').sub.4-x

wherein R is a monovalent organic moiety selected from the groupconsisting of an alkyl group having 1 to 6 carbon atoms, an allylradical, a vinyl radical, an epoxy-functional organic group and anacryl-functional organic group. R' is an alkyl radical having 1 to 3carbon atoms and x is an integer having a value of 1 to 3 inclusive;(II) from 13 to 60 mole percent of an organotitanate having the formula

    Ti(OR'').sub.4

wherein R'' is an alkyl radical having 1 to 8 carbon atoms; and (III)from 12 to 60 mole percent of a tin salt of a carboxylic acid having 2to 18 carbon atoms.

The present invention further relates to a method for overcoating asilicone substrate with a paint comprising first coating said siliconesubstrate with the above described primer, thereby forming a primedsilicone substrate, and then overcoating said primed silicone substratewith said paint.

DETAILED DESCRIPTION OF THE INVENTION

Component (I) of the primer compositions of the present invention is analkoxysilane, or a mixture of alkoxysilanes, each alkoxysilane havingthe general formula

    R.sub.x SI(OR').sub.4-x

wherein R is a monovalent organic moiety independently selected from thegroup consisting of an alkyl group having 1 to 6 carbon atoms, an allylradical, a vinyl radical, an epoxy-functional organic group and anacryl-functional organic group, R' is an alkyl radical having 1 to 3carbon atoms and x is an integer having a value of 1 to 3 inclusive. Itis preferred that component (I) is a trialkoxysilane (i.e., x=1), mostpreferably a trimethoxysilane.

For the purposes of the present invention, when R is the above mentionedepoxy-functional organic group, it is attached to the silicon atom by asilicon-carbon bond, the organic portion acting only as a connectinggroup between the epoxy functionality and the silicon atom of thesilane. The nature of the connecting group is thus not critical as longas it contains no more than about 6 carbon atoms and it contains noother functionality which is reactive with components (II) and (III) ofthe invention, described infra. As will be apparent to the skilledartisan, this connecting group must also not adversely affect the methodof the present invention wherein a paint or other coating is applied toa silicone substrate primed with the compositions of the invention.Examples of suitable connecting groups include alkylene groups, such astrimethylene, tetramethylene and hexamethylene, and oxygen-linkedalkylene groups, such as oxypropylene and oxybutylene. Specificepoxy-functional alkoxysilanes includeglycidoxypropyldimethylmethoxysilane andglycidoxypropylmethyl-di-isopropoxysilane. A particularly preferredepoxy-functional alkoxysilane of the invention isgamma-glycidoxypropyltrimethoxysilane.

Similarly, when R is the above mentioned acryl-functional organic group,it is attached to the silicon atom through a silicon-carbon bond whereinthe nature of the organic connecting group is again not critical as longas it contains no more than about 6 carbon atoms and does not containany functionality which can react adversely with the other components ofthe compositions and method of the instant invention. Thus, theconnecting groups described above for the epoxy-functional organic groupare also suitable in the acryl-functional silanes. As used herein, theterm "acryl" refers to a moiety having the structure

    CH.sub.2 ═C(Q)C(O)O--

in which Q is selected from the group consisting of hydrogen and analkyl radical having 1 to 6 carbon atoms. Preferred alkoxysilanes havingsuch acryl functionality include acryloxypropyltrimethoxysilane andmethacryloxypropyltrimethoxysilane.

Specific examples of other alkoxysilanes which are suitable for use ascomponent (I) include methyltrimethoxysilane, vinyltrimethoxysilane,allyltrimethoxysilane, butyltrimethoxysilane, hexyltrimethoxysilane,vinyltriethoxysilane, allyltriethoxysilane, methyltriethoxysilane,dimethyldimethoxysilane, methylvinyldimethoxysilane andmethylallyldimethoxysilane.

Component (II) of the present invention is an organotitanate having theformula

    Ti(OR'').sub.4

wherein R'' is an independently selected alkyl radical having 1 tocarbon atoms. Specific examples of suitable organotitanates includetetrabutyl titanate, tetraisopropyl titanate, tetramethyl titanate,ethylmethyldibutyl titanate, tetraoctyl titanate and tetraethylhexyltitanate. In preparing the primer compositions of the present invention,it is preferred that component (II) is either tetra(n-)butyl titanate ortetraisopropyl titanate.

Surprisingly, it has been found that chelated organotitanates, such astitanium isopropoxybis(acetylacetonate), result in the formation ofundesirable precipitates when mixed with components (II) and (III),described infra. Therefore, even though such titanium compounds havebeen successfully employed in various primer compositions of the priorart, they are not within the scope of the present invention.

Component (III) of the present invention is a tin (II) or tin (IV) saltof at least one carboxylic acid having 2 to 18 carbon atoms, theremaining valences of the tin being satisfied by a moiety selected fromthe group consisting of alkyl radicals having 1 to 4 carbon atoms and aphenyl radical. Examples of suitable tin (IV) compounds includedibutyltin diacetate, dibutyltin dilaurate and tin tripropyl acetate.Examples of tin (II) compounds include stannous octoate, stannousoxalate, stannous caprylate, stannous 2-ethylhexoate, stannousnaphthanate, stannous oleate, stannous palmitate and stannous stearate.

The above described components (I), (II) and (III) of the presentinvention are well known in the art, many of them being commerciallyavailable, and no further description thereof is considered necessary toenable one of ordinary skill in the art to practice the invention.

In order to prepare the primer compositions of the present invention,from about 25 to about 75 mole percent of component (1), from about 13to about 60 mole percent of component (II) and from about 12 to about 60mole percent of component (III) are thoroughly blended to form ahomogeneous dispersion or solution. It has been found that primercompositions outside these critical ranges have a significantly reducedability to promote adhesion between a silicone substrate coated with theprimer composition and a subsequently applied paint or overcoat layer.In highly preferred embodiments, the relative molar percentages ofcomponents (I), (II) and (III) are 48 to 65, 20 to 36 and 15 to 31,respectively.

Although the above described primer composition can be applied (i.e.,coated) directly to a silicone substrate at 100% solids, it is preferredto dilute the composition with one or more organic solvents in order toreduce application viscosity and limit the thickness of the primer coat.Examples of suitable solvents for this purpose are hexane, heptane,toluene, xylene, mineral spirits and cyclic siloxanes, heptane beingpreferred. When a solvent or solvent mixture is employed, it ispreferred that from about 0.5 to about 10 weight percent of the abovedescribed primer composition is thoroughly dispersed therein.

In addition to the solvent, it is contemplated that the primercompositions of the present invention can further comprise minorportions (e.g., up to about 5 parts by weight per 100 parts by weight ofsaid component I, II and III) of dyes, pigments, flow additive, and thelike.

In order to use the above described primer composition according to themethod of the present invention, the primer composition may first beapplied to a silicone substrate by the usual techniques practiced in theart, such as dip coating, spray painting, knife coating, brush coating,inter alia. As used herein, the term "silicone substrate" is intended toencompass both silicone homopolymer compositions and organic-siliconecopolymer compositions and includes such substrates as silicone rubbers,silicone sealants, silicone resins, silicone-alkyd copolymercompositions, silicone-epoxy copolymer compositions, silicone-urethanecopolymer compositions, and the like. However, it has been observed thatnot all types of silicone substrates can be effectively primed with thecompositions of the invention. A preferred silicone substrate which maybe primed with the instant compositions to illustrate the unexpectedlysuperior performance thereof is a cured product based on siliconesystems taught in U.S. Pat. No. 4,537,829 to Blizzard et al., whichpatent is assigned to the assignee of the present invention and ishereby incorporated by reference. Briefly stated, these curablecompositions comprise a blend of (A) from 1 to 200 parts by weight of aliquid organosilicon resin, (B) 100 parts by weight of a vinyl orhydroxyl-functional organosilicon polymer, (C) from 1 to 50 parts byweight of a vinylated organosilicon resin and (D) from 0.00003 to 0.035parts by weight of a hydrosilylation catalyst. The above named component(A) is a reaction product of (i) an organosilicon resin consistingessentially of triorganosiloxy units and SiO₂ units in a molar ratio of0.6 to 0.9 and (ii) a polyorganohydrogensiloxane. Component (B) is anorganosilicon polymer having the formula

    R''R'''.sub.2 SiO(R'''.sub.2 SiO).sub.y SiR'''.sub.2 R''

wherein each R''' is selected from the group consisting of monovalenthydrocarbon radicals, each R'' is selected from the group consisting ofOH radicals and R''' radicals, y has a value of 0 to 5000, there beingon average at least two radicals of the organosilicon polymer selectedfrom the group consisting of vinyl radicals and hydroxyl radicals.Component (C) in the above composition is an organosilicon resinconsisting essentially of Me₂ (CH₂ ═CH)SiO1/2, Me₃ SiO_(1/2) units andSiO_(4/2) units in a molar ratio of 0.1:0.6:1 to 0.25:0.9:1.respectively, wherein Me hereinafter denotes a methyl radical.

Another preferred silicone substrate is a cured elastomer based on ahigh molecular weight vinyl-functional silicone gum (e.g., one having aviscosity of at least about 10⁴ Poise at 25° C.) which contains fromabout 10 to about 40 parts by weight of a silica filler having a surfacearea between about 50 and 300 m² /g. These materials are well known inthe art, are available commercially and are generally cured with the aidof a peroxide catalyst.

After the primer has dried on the silicone substrate for about 15minutes to about 24 hours and essentially all of the dilution solventhas evaporated therefrom, the primed silicone substrate is overcoated orpainted with a conventional coating or paint composition. The lattermaterial may be selected from organic or silicone systems orcompositions based on copolymers thereof. Thus, for example, theovercoat may comprise a formulated silicone resin paint, an alkyd paint,a polyurethane paint or a silicone-alkyd paint, among others. After thepaint or coating has been applied and dried and/or cured onto the primedsilicone substrate, an improved degree of adhesion between the paint orcoating and the silicone substrate is obtained. A paint which derives aparticular advantage in this manner is one based on a silicone-alkydcopolymer and has been effectively employed as a maintenance coating fornaval vessels, wherein durability and good adhesion to the overcoatedsubstrate is critical. Other paints or coatings can be based on, e.g.,polyimide or epoxy polymers.

EXAMPLES

The following examples are presented to further illustrate the primercompositions and method of the invention, but are not to be construed aslimiting the invention, which is delineated in the appended claims. Allparts and percentages in the examples are on a weight basis and allmeasurements were obtained at 25° C., unless indicated to the contrary.

The following materials, listed alphabetically for ease of reference,were employed in the examples:

ATMS=Allyltrimethoxysilane.

DBTDA=dibutyltin diacetate.

DBTDL=dibutyltin dilaurate.

IBTMS=isobutyltrimethoxysilane.

MTMS=methyltrimethoxysilane.

TBT=tetra(n-)butyl titanate.

TPT=tetraisopropyl titanate.

VTMS=vinyltrimethoxysilane.

Z-6020=An alkoxysilane consisting essentially ofN-(beta-aminoethyl)-gamma-aminopropyltrimethoxysilane; marketed by theDow Corning Corp., Midland, Mich.

Z-6030=An alkoxysilane consisting essentially ofgamma-methacryloxypropyltrimethoxysilane; marketed by the Dow CorningCorp.

Z-6040=An alkoxysilane consisting essentially ofgamma-glycidoxypropyltrimethoxysilane; marketed by the Dow Corning Corp.

EXAMPLES 1-25

Primer compositions of the invention and comparative compositions wereprepared by thoroughly mixing the components (I), (II) and (III) shownin Table 1 in the molar ratios indicated. Each primer composition wasdiluted with heptane to provide an approximately 10 weight percentdispersion therein, the following being exceptions: the compositions ofExamples 9-11 and 15 as well as (Comparative) Examples 22-24 werediluted to form 4% dispersions in heptane and Examples 13-14 werediluted to form 12% dispersions in heptane.

A curable silicone rubber coating formulation was prepared by thoroughlymixing equal weights of the following two components according to theteachings of above cited U.S. Pat. No. 4,537,829 to Blizzard et al. Thefirst component consisted of a mixture of 82 weight percent of adimethylvinylsiloxy endblocked polydimethylsiloxane having a viscosityof about 3 Pa's and 18 weight percent of a benzene soluble resincopolymer of triorganosiloxy units and SiO₂ units in the molar ratio ofabout 0.7 mole of triorganosiloxy units per mole of SiO₂ units where thetriorganosiloxy units were trimethylsiloxy units and dimethylvinylsiloxyunits and the resin copolymer contained about 2 weight percentsilicon-bonded vinyl radicals. The second component of the siliconecoating composition was a blend of 91.3 weight percent of a liquidorganosilicon resin as shown in Example 1 of U.S. Pat. No. 4,537,829 (atcolumn 8, lines 23-44), 0.5 weight percent of 3.5 dimethyl-1-hexyn-3-oland 8.2 weight percent of a mixture of methylvinylcyclosiloxanes.

The above curable silicone rubber mixture was catalyzed with a platinumcomplex hydrosilation catalyst (53 ppm platinum based on the weight ofthe total coating mixture). The catalyzed system was coated onto steelpanels and cured thereon at room temperature for at least 24 hours.

Heptane dispersions of the primer composition described in Table 1 werewiped onto the panels coated with the cured silicone rubber using acheesecloth applicator and the resulting film was allowed to air dry forabout 30 minutes. At this point, the primed panels were overcoated witha flat grey silicone-alkyd paint obtained from Seagrave Coatings Corp.of Virginia (Portsmouth. Va.). This paint, described as product numberTT-E-490, is said to meet Military Specification Mil-C-83286B. Afterbeing painted in this manner, each panel was again allowed to dry, thistime for about 72 hours, before being tested.

Bonding of the paint to the primed silicone rubber was evaluated by astandard ASTM D-3359 crosshatch adhesion test. Briefly stated, thisprocedure consists of scribing a square grid onto the coated substratewith a special cutter, applying an adhesive tape to the scribed area andpeeling the tape off. The adhesive tape tends to pull off the coatingand the amount of the scribed coating remaining is an indication of theintegrity of its bond to the substrate beneath. For the purposes herein,the following rating scheme was used:

    ______________________________________                                        Rating   Percent of Scribed Surface Removed By Tape                           ______________________________________                                        0        .sup.˜ 100 (i.e., essentially no adhesion)                     1         .sup.˜ 80                                                     2         .sup.˜ 60                                                     3         .sup.˜ 40                                                     4         .sup.˜ 20                                                     5         .sup.˜ 0 (i.e., approximately 100 adhesion)                   ______________________________________                                    

The results of these adhesion tests are presented in Table 1, from whichit can be seen that primer compositions not within the critical range ofcomponents (I), (II) and (III) of the present invention had ratings ofno more than 3+ (corresponding to about 35% of paint removed by tape)while the primers of the invention all had ratings of at least 4-(corresponding to about 25% of paint removed by tape). It is furthernoteworthy that the aforementioned composition of Fey et al. (expressedin molar ratios in Comparative Example 25), had an adhesion rating ofonly 2.

                                      TABLE 1                                     __________________________________________________________________________            Primer Mixture    Mole Ratio                                                  Component                                                                           Component                                                                           Component                                                                           of Components                                                                         Adhesion                                            (I)   (II)  (III) (I):(II):(III)                                                                        Rating                                      __________________________________________________________________________    Example                                                                        1      ATMS  TBT   DBTDA 52:24:24                                                                              5                                            2      "     "     "     58:24:18                                                                              4+                                           3      "     "     "     42:39:19                                                                              4-                                           4      "     "     "     41:30:29                                                                              4+                                           5      "     "     "     41:20:39                                                                              4+                                           6      "     "     "     27:60:13                                                                              4+                                           7      "     "     "     29:36:35                                                                              4                                            8      "     "     "     27:13:60                                                                              4                                            9      "     "     DBTDL 57:28:15                                                                              5                                           10      "     TPT   "     55:31:14                                                                              4                                           11      "     "     DBTDA 49:28:23                                                                              5                                           12      Z-6030                                                                              TBT   "     41:30:29                                                                              4                                           13      MTMS  "     "     56:22:22                                                                              5                                           14      Z-6040                                                                              "     "     42:29:29                                                                              4                                           15      VTMS  TPT   DBTDL 57:30:13                                                                              4                                           (Comparative)                                                                 Example                                                                       16      ATMS  TBT   DBTDA 83:9:8  3                                           17      "     "     "     92:5:3  3                                           18      "     "     "     60:29:11                                                                              3+                                          19      "     "     "     61:11:28                                                                              3                                           20      "     "     "     76:12:12                                                                              2-3                                         21      Z-6020                                                                              "     "     44:28:28                                                                              1*                                          22      VTMS  --    --    100:0:0 1                                           23      --    --    DBTDA 0:0:100 1                                           24      --    TBT   --    0:100:0 2                                           25      IBTMS TPT   DBTDA 92:6:2  2                                           Control --    --    --    --      0                                           __________________________________________________________________________     *Formed a precipitate.                                                   

EXAMPLE 26

In a procedure similar to that described for Examples 1-25, a 100%solids primer was prepared (i.e., one containing no solvent) having amole ratio of ATMS:TBT:DBTDA of 52:24:24. This primer was applied to thesilicone rubber substrate, as described above, allowed to air dry for 15minutes and then coated with the TT-E 490 Navy Grey paint. This coatingwas air dried for seven days. An adhesion rating of 5 resulted.

COMPARATIVE EXAMPLE 27

A primer mixture consisting of ATMS, titanium acetylacetonate and DBTDAin a molar ratio of 52:24:24 was diluted to form a 12% dispersion inheptane. The titanium acetylacetonate used was an isopropyl alcoholchelate obtained from E. I. du Pont (Wilmington, Del.) under the tradename of TYZOR™TAA. This primer composition formed a precipitate andcould not be readily applied to the silicone rubber substrate.

EXAMPLE 28

The above procedures were repeated wherein a peroxide-cured siliconerubber, based on a copolymer of a polydimethylsiloxane gum having about0.14 mole percent of methylvinylsiloxane units and filled with about 31weight percent of a pyrogenic silica having an approximate surface areaof 255 m² /g, was wiped with a primer having the composition shown inExample 1 (diluted to a 11.9% dispersion in heptane). After drying forabout 30 minutes, the primed silicone rubber was overcoated with theabove described TT-E 490 and with a commercial spray paint (KRYLO™Crystal Clear 1301 acrylic; Borden Inc., Columbus, Ohio). Upon furtherdrying, these coated substrates were subjected to the crosshatchadhesion test and resulted in ratings of 5 in each case. Similarlypainted unprimed controls using this rubber substrate each had anadhesion rating of 0.

COMPARATIVE EXAMPLES 29-30

The experiment of Example 28 was repeated using two room temperaturevulcanizing (RTV) silicone compositions, each of which was based on avinyl-terminated polydimethylsiloxane liquid,methylvinylcyclopolysiloxane and a polyfunctional SiH-functionalcrosslinker. The first of these RTVs was filled with about 12.4 weightpercent of a pyrogenic silica having a surface area of about 255 m² /gwhile the second RTV contained about 38 weight percent of a mixture of65 percent by weight of dimethylvinylsiloxy endblockedpolydimethylsiloxane oil and 35 percent by weight of a benzene solubleresin copolymer of triorganosiloxy units and SiO₂ units having a ratioof about 0.7 mole of triorganosiloxy unit per mole of SiO₂ unit wherethe triorganosiloxy units are trimethylsiloxy units anddimethylvinylsiloxy units and the resin copolymer has about 2 weightpercent silicon-bonded vinyl radicals. Each of these RTV compositionswas catalyzed with platinum, coated onto a steel panel and cured.

A primer having the composition shown in Example 1 was applied to eachof the above cured silicone RTV substrates, dried for 30 minutes andovercoated with the TT-E 490 and the KRYLO™ paints. After the paintswere dried for 72 hours, each crosshatch adhesion test resulted in arating of 3 for the case of the first silicone RTV substrate and arating of 0 for the second silicone RTV substrate. The unprimed controlsgave ratings of 0 in each instance. This series of experiments indicatesthat the unique adhesion promoting character of the instant primercompositions is not of universal utility for all silicone substrates.Rather, it is specific to at least the types of silicone surfacesillustrated in Examples 1-15, 26 and 28.

I claim:
 1. A primer composition consisting essentially of a mixture of(I) from 25 to 75 mole percent of at least one alkoxysilane having the general formula

    R.sub.x Si(OR').sub.4-x

wherein R is a monovalent organic moiety selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, an allyl radical, a vinyl radical, an epoxy functional organic group and an acryl-functional organic group, R' is an alkyl radical having 1 to 3 carbon atoms and x is an integer having a value of 1 to 3 inclusive; (II) from 13 to 60 mole percent of an organotitanate having the formula

    Ti(OR'').sub.4

wherein R'' is an alkyl radical having 1 to 8 carbon atoms; and (III) from 12 to 60 mole percent of a tin salt of a carboxylic acid having 2 to 18 carbon atoms.
 2. The composition according to claim 1, wherein x of said alkoxysilane (I) is
 1. 3. The composition according to claim 2, wherein R' of said alkoxysilane (I) is a methyl radical.
 4. The composition according to claim 3, wherein said alkoxysilane (I) is selected from the group consisting of allyltrimethoxysilane, vinyltrimethoxysilane, methyl trimethoxysilane, gamma-glycidoxypropyltrimethoxysilane, acryloxypropyltrimethoxysilane and methacryloxypropyltrimethoxysilane.
 5. The composition according to claim 4, wherein said organotitanate (II) is selected from the group consisting of tetrabutyl titanate and tetraisopropyl titanate.
 6. The composition according to claim 5, wherein said tin salt (III) is selected from the group consisting of dibutyltin diacetate and dibutyltin dilaurate.
 7. The composition according to claim 6, wherein said alkoxysilane (I) is allyltrimethoxysilane and the molar percentages of said alkoxysilane (I), said organotitanate (II) and said tin salt (III) are 48 to 65, 20 to 36 and 15 to 31, respectively.
 8. A primer composition consisting essentially of:(i) a mixture of(I) from 25 to 75 mole percent of at least one alkoxysilane having the general formula

    R.sub.x Si(OR').sub.4-x

wherein R is a monovalent organic moiety selected from the group consisting of an alkyl group having 1 to 6 carbon atoms, an allyl radical, a vinyl radical, an epoxy-functional organic group and an acryl-functional organic group, R' is an alkyl radical having 1 to 3 carbon atoms and x is an integer having a value of 1 to 3 inclusive; (II) from 13 to 60 mole percent of an organotitanate having the formula

    Ri(OR'').sub.4

wherein R'' is an alkyl radical having 1 to 8 carbon atoms; and (III) from 12 to 60 mole percent of a tin salt of a carboxylic acid having 2 to 18 carbon atoms, and (ii) from 90 to 99.5 weight percent of an organic solvent based on the weight of said mixture (i).
 9. The composition according to claim 8, wherein x of said alkoxysilane (I) is
 1. 10. The composition according to claim 9, wherein R' of said alkoxysilane (I) is a methyl radical.
 11. The composition according to claim 10, wherein said alkoxysilane (I) is selected from the group consisting of allyltrimethoxysilane, vinyltrimethoxysilane, methyl trimethoxysilane, gamma-glycidoxypropyltrimethoxysilane, acryloxypropyltrimethoxysilane and methacryloxypropyltrimethoxysilane.
 12. The composition according to claim 11, wherein said organotitanate (II) is selected from the group consisting of tetrabutyl titanate and tetraisopropyl titanate.
 13. The composition according to claim 12, wherein said tin salt (III) is selected from the group consisting of dibutyltin diacetate and dibutyltin dilaurate.
 14. The composition according to claim 13, wherein said alkoxysilane (I) is allyltrimethoxysilane and the molar percentages of said alkoxysilane (I), said organotitanate (II) and said tin salt (III) in said mixture (i) are 48 to 65, 20 to 36 and to 31, respectively. 